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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531656Generated: November 1, 2026

Water → HCID 21249983, compound

https://huagongshe.com/reaction/1531656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantCyclopropanecarbonyl chlorideHCID 77637—
ReactantHCID 21249973HCID 21249973—
SolventBenzeneHCID 241—
ProductHCID 21249983HCID 21249983—

Reaction Steps

0.5 g of 7-bromo-1-(4-nitrophenyl)-4-methyl-8-methoxy-5H-2,3-benzodiazepine (Example 3, Step C) is suspended in 15 ml of benzene, mixed with 0.53 g of potassium carbonate and 0.17 ml of cyclopropylcarboxylic acid chloride and then refluxed for 5 hours. Then, the mixture is stirred with water, the organic phase is separated, washed in succession with soda solution and water, dried, filtered and concentrated by evaporation. The residue is purified by absorptive precipitation in ethanol, and 0.38 g of 7-bromo-3-cyclopropylcarbonyl-1-(4-nitrophenyl)-4-methyl-8-methoxy-3H-2,3-benzodiazepine of the title compound with a melting point of 231-223° C. is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06200970B1
Source datasetuspto-grants-2001_03
ORD IDord-6d546301daec4266a05d92c60bc47078
Source noteuspto-grants-2001_03